Reacción #95743

ord-a08aa8233f444ca6903547a37a2547e2

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaheated
  2. 2
    Temperaturaunder reflux for 0.5 hour
  3. 3
    TemperaturaAfter cooling
  4. 4
    Filtraciónthe separated material is filtered off under suction
  5. 5
    Otrorecrystallised
  6. 6
    Otroform ethanol

Procedimiento

4.1 g of ethyl α-amino-1,3,4,5-tetrahydro-5-oxo-2H-1,4-benzodiazepin-2-ylidene-acetate are dissolved in 25 ml of ethyl acetate, treated with 3.1 ml (18.1 mmol) of N,N-dimethylformamide diethyl acetal and heated to boiling under reflux for 0.5 hour. After cooling, the separated material is filtered off under suction and recrystallised form ethanol. After chromatography of the mother liquor, there is obtained a second portion of ethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate of the same purity; melting point 166°-168° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04346034uspto-grants-1982_08